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- source_evidence_literature type ECO_0000212 NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_assertion description "[However, since the first identification of autosomal recessive (AR), X-linked recessive (XR) and AD PID-causing genes in 1985 (ADA; severe combined immunodeficiency), 1986 (CYBB, chronic granulomatous disease) and 1989 (SERPING1; hereditary angioedema), respectively, the number of genetically defined AD PIDs has increased more rapidly than that of any other type of PID.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_assertion evidence source_evidence_literature NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_assertion SIO_000772 25645939 NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_assertion wasDerivedFrom befree-2016 NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_assertion wasGeneratedBy ECO_0000203 NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1260494.RA_nvfM5pUsI9Tl_zWDBIzRdeB02WO81tO2BNKneV11vg130_provenance.